Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code: OPT-R-1000 The OrthoPAT Recalled by Haemonetics Corporation Due to OrthoPAT¿ reservoirs are missing the cannula inside the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Haemonetics Corporation directly.
Affected Products
Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code: OPT-R-1000 The OrthoPAT orthopedic perioperative autotransfusion system indicated for use to salvage RBCs from blood lost intraoperatively and postoperatively during surgical procedures
Quantity: 348 units
Why Was This Recalled?
OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The absence of this cannula prevents the emptying of blood from the reservoirs. The inability to empty the reservoir means that the collected blood cannot be processed.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Haemonetics Corporation
Haemonetics Corporation has 31 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report